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Please use this identifier to cite or link to this item: http://dspace.ucuenca.edu.ec/handle/123456789/34244
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dc.contributor.authorClos, Victoria-
dc.contributor.authorVander Heyden, Yvan-
dc.contributor.authorWilches Arizabala, Isabel Maria-
dc.contributor.authorJerves Andrade, Maria De lourdes-
dc.contributor.authorPeñaherrera Wilches, Eugenia-
dc.contributor.authorJimenez Castillo, Priscilla Yazmin-
dc.contributor.authorJiménez Altayó, Francesc-
dc.contributor.authorCuzco Quizhpi, Nancy Mirian-
dc.contributor.authorVila Calsina, Elisabet Null-
dc.contributor.authorTobar Solano, Vladimiro Alexis-
dc.contributor.authorLeon Tamariz, Fabian-
dc.date.accessioned2020-05-08T00:21:54Z-
dc.date.available2020-05-08T00:21:54Z-
dc.date.issued2019-
dc.identifier.issn1478-6419-
dc.identifier.urihttp://dspace.ucuenca.edu.ec/handle/123456789/34244-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85066777908&origin=inward-
dc.descriptionAerial parts (leaves, flowers, stem) of Peperomia galioides extract administered to mice, was used to confirm its anti-inflammatory and sedative folk uses. The anti-inflammatory activity was assessed by croton oil-induced ear oedema and myeloperoxidase (acute inflammation); cotton pellet-induced granuloma (sub-acute inflammation) and Escherichia coli Lipopolysaccharide (LPS) induced inflammation (cellular mediators). The sedative activity was studied by the pentobarbital-induced sleeping time test. Single doses (300 and 600 mg/kg; i.p.) of the extract reduced croton oil-induced ear oedema and myeloperoxidase activity. Six days administration of the extract (300 mg/kg, i.p.) to mice implanted with cotton pellets diminished granuloma formation. LPS (20 mg/kg, i.p.) enhanced plasma nitrites and TNF-α levels that were inhibited by the extract. The duration but not the onset of sleeping time was enhanced by 300 and 600 mg/kg of the extract. Our results show that P. galioides has anti-inflammatory and sedative activities in mice, which validates its traditional use.-
dc.description.abstract© 2019, © 2019 Informa UK Limited, trading as Taylor & Francis Group. Aerial parts (leaves, flowers, stem) of Peperomia galioides extract administered to mice, was used to confirm its anti-inflammatory and sedative folk uses. The anti-inflammatory activity was assessed by croton oil-induced ear oedema and myeloperoxidase (acute inflammation); cotton pellet-induced granuloma (sub-acute inflammation) and Escherichia coli Lipopolysaccharide (LPS) induced inflammation (cellular mediators). The sedative activity was studied by the pentobarbital-induced sleeping time test. Single doses (300 and 600 mg/kg; i.p.) of the extract reduced croton oil-induced ear oedema and myeloperoxidase activity. Six days administration of the extract (300 mg/kg, i.p.) to mice implanted with cotton pellets diminished granuloma formation. LPS (20 mg/kg, i.p.) enhanced plasma nitrites and TNF-α levels that were inhibited by the extract. The duration but not the onset of sleeping time was enhanced by 300 and 600 mg/kg of the extract. Our results show that P. galioides has anti-inflammatory and sedative activities in mice, which validates its traditional use.-
dc.language.isoes_ES-
dc.sourceNatural Product Research-
dc.subjectPeperomia galioides-
dc.subjectSedative activity-
dc.subjectAnti-inflammatory-
dc.subjectmice models-
dc.subjectsedative activity-
dc.subjectanti-inflammatory-
dc.subjectmice models-
dc.subjectPeperomia galioides-
dc.titleAnti-inflammatory and sedative activities of Peperomia galioides: in vivo studies in mice-
dc.typeARTÍCULO-
dc.ucuenca.idautor0000-0002-7788-9886-
dc.ucuenca.idautorAAH961467-
dc.ucuenca.idautor0102286549-
dc.ucuenca.idautor1104122765-
dc.ucuenca.idautor0301624854-
dc.ucuenca.idautor0000-0002-7389-3351-
dc.ucuenca.idautor0000-0002-9034-2041-
dc.ucuenca.idautor0102452075-
dc.ucuenca.idautor0101660579-
dc.ucuenca.idautor0300969334-
dc.ucuenca.idautor0102311610-
dc.identifier.doi10.1080/14786419.2019.1622104-
dc.ucuenca.embargoend2050-12-31-
dc.ucuenca.versionVersión publicada-
dc.ucuenca.embargointerno2050-12-31-
dc.ucuenca.areaconocimientounescoamplio05 - Ciencias Físicas, Ciencias Naturales, Matemáticas y Estadísticas-
dc.ucuenca.afiliacionJiménez, F., Universitat de Barcelona, Barcelona, España-
dc.ucuenca.afiliacionLeon, F., Universidad de Cuenca, Cuenca, Ecuador-
dc.ucuenca.afiliacionVander, Y., Vrije Universiteit Brussel, Elsene, Belgica-
dc.ucuenca.afiliacionTobar, V., Universidad de Cuenca, Cuenca, Ecuador-
dc.ucuenca.afiliacionJerves, M., Universidad de Cuenca, Cuenca, Ecuador-
dc.ucuenca.afiliacionPeñaherrera, E., Universidad de Cuenca, Cuenca, Ecuador-
dc.ucuenca.afiliacionClos, V., Universitat de Barcelona, Barcelona, España-
dc.ucuenca.afiliacionCuzco, N., Universidad de Cuenca, Facultad de Ciencias Químicas, Cuenca, Ecuador-
dc.ucuenca.afiliacionJimenez, P., Universidad de Cuenca, Facultad de Ciencias Químicas, Cuenca, Ecuador-
dc.ucuenca.afiliacionWilches, I., Universidad de Cuenca, Facultad de Ciencias Químicas, Cuenca, Ecuador-
dc.ucuenca.afiliacionVila, E., Universidad de Cuenca, Cuenca, Ecuador; Vila, E., Universitat de Barcelona, Barcelona, España-
dc.ucuenca.correspondenciaVila Calsina, Elisabet Null, elisabet.vila@uab.cat-
dc.ucuenca.volumenVolumen 0-
dc.ucuenca.indicebibliograficoSCOPUS-
dc.ucuenca.factorimpacto0.6-
dc.ucuenca.cuartilQ2-
dc.ucuenca.numerocitaciones0-
dc.ucuenca.areaconocimientofrascatiamplio1. Ciencias Naturales y Exactas-
dc.ucuenca.areaconocimientofrascatiespecifico1.4 Ciencias Químicas-
dc.ucuenca.areaconocimientofrascatidetallado1.4.1 Química Orgánica-
dc.ucuenca.areaconocimientounescoespecifico051 - Ciencias Biológicas y Afines-
dc.ucuenca.areaconocimientounescodetallado0512 - Bioquímica-
dc.ucuenca.urifuentehttps://www.tandfonline.com/toc/gnpl20/current-
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